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Structure of 1240621-87-7
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2-Bromopyrimidin-5-ol features a bromine atom at the 2-position and a hydroxyl group at the 5-position on a pyrimidine core, delivering high reactivity in nucleophilic substitution and coupling processes. This bench-stable compound integrates readily into heterocyclic scaffolds, serving as a key intermediate in medicinal chemistry and agrochemical synthesis.
2-Bromopyrimidin-5-ol serves as a versatile building block in medicinal chemistry, enabling efficient late-stage functionalization via palladium-catalyzed cross-coupling reactions. Its bromine atom facilitates C–C and C–heteroatom bond formation under mild conditions, while the pyrimidine ring provides structural rigidity and hydrogen-bonding capability. The compound exhibits good bench stability and compatibility with diverse functional groups, making it suitable for modular synthesis of bioactive heterocycles and API intermediates.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: